Browsing Tag
United States Food and Drug Administration
193 posts
Aurobindo Pharma stock slips as USFDA OAI classification tests investor confidence in #AUROPHARMA
Aurobindo Pharma faces USFDA OAI pressure at a Telangana unit. Find out why this matters for #AUROPHARMA investors today!
May 25, 2026
Accro Bioscience raises $50m Series C to advance AC-101 and immune-mediated disease pipeline
Ulcerative colitis needs safer oral options. Accro’s OrbiMed-led raise puts RIPK2 inhibition under a bigger clinical spotlight.
May 19, 2026
Citius Oncology (CTOR) balances LYMPHIR launch momentum with cash runway pressure after Q2 loss
Citius Oncology has LYMPHIR revenue, but cash runway only reaches November 2026. Investors now face launch proof versus dilution risk.
May 16, 2026
Is biomarker-driven approval the breakthrough ALS drug development has been waiting for?
Can neurofilament light fast-track ALS drug approvals? Explore how Clene Inc.’s FDA signal could reshape timelines, risk, and competition.
May 6, 2026
Citius Oncology (CTOR) stock in focus as $36.5m financing targets LYMPHIR commercialization
Citius Oncology has capital and an approved CTCL drug. The harder question is whether LYMPHIR can turn niche oncology promise into revenue.
May 6, 2026
Syntara Limited raises A$8m as ASX:SNT advances amsulostat toward Phase 2b trial
Syntara has capital, catalysts, and dilution. The real question is whether amsulostat data can shift investor trust in ASX:SNT.
April 29, 2026
Seaport Therapeutics seeks $212m IPO as neuropsychiatry biotech window reopens
Seaport’s IPO tests biotech appetite before key depression data. Here’s why SPTX, PureTech, and psychiatry investors are watching.
April 28, 2026
Nuvalent (NASDAQ: NUVL) sharpens zidesamtinib case at AACR 2026 with post-TKI ROS1 lung cancer data
Nuvalent’s AACR 2026 zidesamtinib data could reshape the ROS1 NSCLC treatment debate ahead of its FDA decision. Read what it means now.
April 19, 2026
Could Pixclara become the missing imaging tool in U.S. glioma care after FDA NDA acceptance?
Could Pixclara transform U.S. glioma imaging after FDA NDA acceptance? Explore what Telix Pharmaceuticals Limited’s September catalyst could change next.
April 12, 2026
Replimune Group (NASDAQ: REPL) plans layoffs after FDA rejects Tudriqev again, forcing a biotech reset
Replimune plans layoffs after the FDA rejected Tudriqev again. Read what the setback means for REPL stock, cash runway, strategy, and rivals.
April 11, 2026